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549 results for “terrestrial isopods”
Figure 1 from: Taiti S, Wynne JJ (2015) The terrestrial Isopoda (Crustacea, Oniscidea) of Rapa Nui (Easter Island), with descriptions of two new species. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 27–49. https://doi.org/10.3897/zookeys.515.9477
Figure 1 - Styloniscus manuvaka sp. n.: A ♀ paratype in dorsal view. Hawaiioscia rapui sp. n.: B ♀ paratype in dorsal view.
Figure 2 from: Sfenthourakis S, Taiti S (2015) Patterns of taxonomic diversity among terrestrial isopods. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 13–25. https://doi.org/10.3897/zookeys.515.9332
Figure 2 - Skewness in the distribution of taxonomic richness with results of the respective Shapiro-Wilks tests. A for number of genera per families B for number of species per genera, and C for number of species per families.
Figure 4 from: Taiti S, Wynne JJ (2015) The terrestrial Isopoda (Crustacea, Oniscidea) of Rapa Nui (Easter Island), with descriptions of two new species. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 27–49. https://doi.org/10.3897/zookeys.515.9477
Figure 4 - Styloniscus manuvaka sp. n., ♂ paratype: A pereopod 1 B pereopod 6 C pereopod 7 D genital papilla and pleopod 1 E pleopod 2.
Figure 3 from: Taiti S, Wynne JJ (2015) The terrestrial Isopoda (Crustacea, Oniscidea) of Rapa Nui (Easter Island), with descriptions of two new species. In: Taiti S, Hornung E, Štrus J, Bouchon D (Eds) Trends in Terrestrial Isopod Biology. ZooKeys 515: 27–49. https://doi.org/10.3897/zookeys.515.9477
Figure 3 - Styloniscus manuvaka sp. n., ♀ paratype: A left mandible B right mandible C maxillula D maxilla E maxilliped.
Figure 5 from: Kashani GM (2016) Iranian terrestrial isopods of the family Cylisticidae Verhoeff, 1949 with a description of a new species (Isopoda, Oniscidea). ZooKeys 582: 157-165. https://doi.org/10.3897/zookeys.582.7199
Figure 5 - Map of Iran with the northern part enlarged, indicating the sampling localities of Cylisticus masalicus. * indicates the type locality.
Figure 4 from: Kashani GM (2016) Iranian terrestrial isopods of the family Cylisticidae Verhoeff, 1949 with a description of a new species (Isopoda, Oniscidea). ZooKeys 582: 157-165. https://doi.org/10.3897/zookeys.582.7199
Figure 4 - Cylisticus masalicus sp. n., male, paratype. A pleopod endopodite I B–C pleopod exopodite I D pleopod II E pleopod exopodite III F pleopod exopodite IV G pleopod exopodite V. Scales = 0.5 mm.
Figure 3 from: Kashani GM (2016) Iranian terrestrial isopods of the family Cylisticidae Verhoeff, 1949 with a description of a new species (Isopoda, Oniscidea). ZooKeys 582: 157-165. https://doi.org/10.3897/zookeys.582.7199
Figure 3 - Cylisticus masalicus sp. n., male, paratype. A cephalon dorsal view B cephalon frontal view C left side of the body showing the position of noduli laterales D antenna E telson and uropods F pereopod I and enlarged carpus and dactylus G pereopod VI and enlarged basis H pereopod VII and enlarged ischium. Scale: 1 mm (A–C); 0.5 mm (D–H).
Figure 1 from: Kashani GM (2016) Iranian terrestrial isopods of the family Cylisticidae Verhoeff, 1949 with a description of a new species (Isopoda, Oniscidea). ZooKeys 582: 157-165. https://doi.org/10.3897/zookeys.582.7199
Figure 1 - Map of Iran with the northern part enlarged, indicating the sampling localities of Cylisticoides angulatus (□ previous records, ■ new records) and Cylisticus rotundifrons (○ previous records, ● new records).
Supplementary material 1 from: Nasu T, Kitagawa K, Karasawa S (2018) Species compositions of terrestrial isopods in public parks of a commuter town in Japan. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 389-399. https://doi.org/10.3897/zookeys.801.21875
AIC values of GLMs at the five apatial scales :
Figure 3 from: Szlavecz K, Vilisics F, Tóth Z, Hornung E (2018) Terrestrial isopods in urban environments: an overview. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 97-126. https://doi.org/10.3897/zookeys.801.29580
Figure 3 Responses of three synanthropic isopod species to urbanization gradient. Each data point is percentage of total number of individuals (N) of a given species caught in pitfall traps. Philosciamuscorum: N = 7473, Porcellioscaber: N = 12314, Armadillidiumvulgare: N = 816. The study was carried out in urban, suburban, and rural forest patches and parks in Sorø, Denmark. Data from Vilisics et al. (2007); original figure.
Figure 3 from: Hassall M, Moss A, Dixie B, Gilroy JJ (2018) Interspecific variation in responses to microclimate by terrestrial isopods: implications in relation to climate change. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 5-24. https://doi.org/10.3897/zookeys.801.24934
Figure 3 Aggregation of isopod species differing in desiccation resistance at different temperatures. Mean ± 1 SE aggregation indices (variance:mean ratio) at 90% relative humidity. aP.scaber (F 4,249 = 3.76, p < 0.01) bA.vulgare (F 4,249 = 1.97, P < 0.01) cO.asellus (F 4, 249 = 12.22, P < 0.001) d thermal reaction norms for aggregation expressed as quadratic response curves for: P.scaber (dashed line): y = -11.519 + 1.526× - 0.04×2; A.vulgare (solid line): y = -3.534 + 0.574× 0.016×2; O.asellus (dotted line): y = -5.890 + 0.814× – 0.018×2.
Figure 4 from: Hassall M, Moss A, Dixie B, Gilroy JJ (2018) Interspecific variation in responses to microclimate by terrestrial isopods: implications in relation to climate change. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 5-24. https://doi.org/10.3897/zookeys.801.24934
Figure 4 Moisture reaction norms for a) sheltering and b) feeding behaviours with changing sand moisture content (time spent in behaviour as percentages of total observed behaviours). Lines represent linear regression models: A.vulgare (solid line) (sheltering: y = 95.24 – 1.05×; feeding: y = 0.32 + 0.03), P.scaber (dashed line) (sheltering: y = 96.72 – 0.19×; feeding: y= 0.22 + 0.05×), Ph.muscorum (dotted line) (sheltering: y = 93.14 – 2.16×; feeding: y = 0.36 + 0.55x). Further regression statistics and number of observations (N), are given in Table 1.
Figure 6 from: Souty-Grosset C, Faberi A (2018) Effect of agricultural practices on terrestrial isopods: a review. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 63-96. https://doi.org/10.3897/zookeys.801.24680
Figure 6 Sampling Philosciamuscorum in wheat (pitfall traps). Importance of hedges and woods for inducing the presence of the species in the studied plots. Key: Dark bar: P.muscorum in the plot. Light gray bar: P.muscorum in the borders of the plot (hedges/wood). Codes were expressed for each plot: the first three letters corresponded to the name of the location, the two following numbers to the French department (16: Charente; 86: Vienne; 79: Deux Sèvres; 36 (1 and 2): Indre).
Figure 9 from: Souty-Grosset C, Faberi A (2018) Effect of agricultural practices on terrestrial isopods: a review. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 63-96. https://doi.org/10.3897/zookeys.801.24680
Figure 9 Density of Armadillidiumvulgare during 3 years in the same field plots. Samples were collected in October of each year before the sowing of summer crops (from Larsen et al. 2007). Abbreviation: GU: ground under.
Figure 3 from: Souty-Grosset C, Faberi A (2018) Effect of agricultural practices on terrestrial isopods: a review. In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 63-96. https://doi.org/10.3897/zookeys.801.24680
Figure 3 Number of isopods collected by hand-searching in three different types of grasslands in western France. The two sites differ in farming intensity: Lusignan has experienced intensive practices over many years, whereas Fors is in a zone of mixed farming, with a more recent history of intensification. Note the different scales in the y axes (from Souty-Grosset et al. 2005a).
Figure 1 from: Shultz JW (2018) A guide to the identification of the terrestrial Isopoda of Maryland, U.S.A. (Crustacea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 207-228. https://doi.org/10.3897/zookeys.801.24146
Figure 1 ACylisticusconvexus, head, dorsoanterior view, antennae removed (based on Schmidt 2008: figure 32) BArmadillidiumvulgare, male pleon, ventral view CPlatyarthrushoffmannseggii (after Hopkin 2014: figure 17) DArmadilloniscusellipticus, insets highlight uropods and antennal flagellum EScyphacellaarenicola, inset highlights antennal flagellum. Abbreviations: a lateral perimeter narrows gradually from pereon to pleon; a1 socket of antenna I; a2 antenna II or socket of antenna II; al anterolateral lobe; b lateral perimeter narrows abruptly from pereon to pleon; ca carina; cd cephalic dorsum; ce compound eye; en endopodite; ex exopodite; fl flagellum; fm frontal margin; frl frontal lamina; lg lung; tg tergite; pe peduncle of antenna II; pp pleopod; pr protopodite; pt pleotelson; ur uropod. Scale bars: 1 mm.
Figure 4 from: Shultz JW (2018) A guide to the identification of the terrestrial Isopoda of Maryland, U.S.A. (Crustacea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 207-228. https://doi.org/10.3897/zookeys.801.24146
Figure 4 Porcellionidae, Trachelipodidae, Cylisticidae. APorcellioscaberBPorcellionidespruinosusCPorcelliospinicornis, head, dorsal view DTrachelipusrathkii, head, dorsal view EPorcelliolaevis, head and first pereonal tergite, dorsal view FCylisticusconvexus, head and first pereonal tergite, dorsal view.
Figure 5 from: Shultz JW (2018) A guide to the identification of the terrestrial Isopoda of Maryland, U.S.A. (Crustacea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 207-228. https://doi.org/10.3897/zookeys.801.24146
Figure 5 Oniscidae, Philosciidae, Halophilosciidae, Ligiidae. AOniscidae: OniscusasellusB–EPhilosciidaeB–CPhilosciamuscorumB dorsal view C pleotelson DChaetophilosciasicula: dorsal view of pleon (after Vandel 1962: figure 247) ELittorophilosciavittata: pleotelson, dorsal view F–GLigiidaeFLigiaexoticaGLigidiumelrodii. Scale bars: 5 mm.
Figure 2 from: Shultz JW (2018) A guide to the identification of the terrestrial Isopoda of Maryland, U.S.A. (Crustacea). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 207-228. https://doi.org/10.3897/zookeys.801.24146
Figure 2 Trichoniscidae. ATrichoniscuspusillusBHaplophthalmusdanicus, highlighting cuticular sculpture of pereon CMiktoniscuscf.medcofi, highlighting cuticular sculpture of pereon D–EMiktoniscusspinosus, male D right pleopod I, ventral view E right pleopod II, ventral view (based on Schultz 1976: figs 8, 9, as M.halophilus) F–GMiktoniscusmedcofi, male: F right pleopod I, ventral view G right pleopod II, ventral view (based on Schultz 1976: figs 40, 41). Abbreviations: en endopodite; ex exopodite. Scale bars: 1 mm.
Figure 2 from: Tajovský K, Štrichelová J, Tuf IH (2018) Terrestrial isopods (Oniscidea) of the White Carpathians (Czech Republic and Slovakia). In: Hornung E, Taiti S, Szlavecz K (Eds) Isopods in a Changing World. ZooKeys 801: 305-321. https://doi.org/10.3897/zookeys.801.24133
Figure 2 The ordination analysis of isopod species recorded at individual study localities in the White Carpathians (CANOCO 5, unconstrained analysis, DCA). For abbreviation of species' names, see Table 2.
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Allen Brain Atlas
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